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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728856Generated: October 30, 2026

Triethyl phosphite → HCID 21667292, compound

https://huagongshe.com/reaction/728856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphiteHCID 31215—
ReactantThionyl bromideHCID 68176—
ReactantHCID 21667325HCID 21667325—
ReactantHCID 53907037HCID 53907037—
ProductHCID 21667292HCID 21667292—

Reaction Steps

The starting material is manufactured as follows: 5-Methyl-5-vinyl-2-oxazoline-4-carboxylic acid ethyl ester, b.p. 65°-75° (13 Pa) is obtained by reaction of isocyanoacetic acid ethyl ester with methyl vinyl ketone in a manner analogous to that described in Example 30. By hydrolysis of the 5-methyl-5-vinyl-2-oxazoline-4-carboxylic acid ethyl ester in a manner analogous to that described in Example 1, 2-formylamino-3-hydroxy-3-methyl-4-pentenoic acid ethyl ester is obtained.Reaction of the 2-formylamino-3-hydroxy-3-methyl-4-pentenoic acid ethyl ester with thionyl bromide and subsequent treatment with triethyl phosphite in a manner analogous to that described in Example 1 yields E-2-formylamino-3-methyl-5-diethylphosphono-3-pentenoic acid ethyl ester in the form of a colourless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05051413
Source datasetuspto-grants-1991_09
ORD IDord-c245f89843804025a501f487a4be5120
Source noteuspto-grants-1991_09